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論文・技術情報

• • Real-world safety profile of sonidegib: a disproportionality analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/11/10
  • A real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) for therapeutic radiopharmaceuticals.
    タグ:

    • FAERS
    2025/11/13
  • Safety of penicillamine and trientine in the treatment of Wilson’s disease: An analysis of the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/11/12
  • Association between immune check point inhibitors and digestive system inflammatory adverse reactions: evidence from pharmacovigilance analysis and systematic review.
    タグ:

    • FAERS
    2025/11/12
  • Drug-induced enterocolitis syndrome with amoxicillin-containing products: A review of cases reported to the FDA adverse event reporting system and published literature.
    タグ:

    • FAERS
    2025/11/11
  • A real-world drug safety surveillance study from the FAERS database of hepatocellular carcinoma patients receiving durvalumab in combination with tremelimumab.
    タグ:

    • FAERS
    2025/11/14
  • Pharmacovigilance analysis of myopathy associated with azoles and nonstatins interactions based on US FAERS database.
    タグ:

    • FAERS
    2025/11/14
  • Mining and analysis of drug-induced shock adverse reactions: A comprehensive pharmacovigilance study based on the US FAERS database.
    タグ:

    • FAERS
    2025/11/13
  • Comparative Renal Safety of Tirzepatide and Semaglutide: An FDA Adverse Event Reporting System (FAERS)-Disproportionality Study.
    タグ:

    • FAERS
    2025/11/13
  • Dysphagia after COVID-19 Vaccination: A Report of Two Cases.
    タグ:

    • VAERS
    • FAERS
    2025/11/13

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